Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.05 (A)
Location

Chromosome 17:50199874 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 6 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 3494 sample genotypes and is mentioned in 1 citation.

Variant displays